435 related articles for article (PubMed ID: 29494651)
1. A streamlined workflow for single-cells genome-wide copy-number profiling by low-pass sequencing of LM-PCR whole-genome amplification products.
Ferrarini A; Forcato C; Buson G; Tononi P; Del Monaco V; Terracciano M; Bolognesi C; Fontana F; Medoro G; Neves R; Möhlendick B; Rihawi K; Ardizzoni A; Sumanasuriya S; Flohr P; Lambros M; de Bono J; Stoecklein NH; Manaresi N
PLoS One; 2018; 13(3):e0193689. PubMed ID: 29494651
[TBL] [Abstract][Full Text] [Related]
2. Genomic Analysis of Circulating Tumor Cells at the Single-Cell Level.
Lu S; Chang CJ; Guan Y; Szafer-Glusman E; Punnoose E; Do A; Suttmann B; Gagnon R; Rodriguez A; Landers M; Spoerke J; Lackner MR; Xiao W; Wang Y
J Mol Diagn; 2020 Jun; 22(6):770-781. PubMed ID: 32247862
[TBL] [Abstract][Full Text] [Related]
3. Chromosomal Instability Estimation Based on Next Generation Sequencing and Single Cell Genome Wide Copy Number Variation Analysis.
Greene SB; Dago AE; Leitz LJ; Wang Y; Lee J; Werner SL; Gendreau S; Patel P; Jia S; Zhang L; Tucker EK; Malchiodi M; Graf RP; Dittamore R; Marrinucci D; Landers M
PLoS One; 2016; 11(11):e0165089. PubMed ID: 27851748
[TBL] [Abstract][Full Text] [Related]
4. A new workflow for whole-genome sequencing of single human cells.
Binder V; Bartenhagen C; Okpanyi V; Gombert M; Moehlendick B; Behrens B; Klein HU; Rieder H; Ida Krell PF; Dugas M; Stoecklein NH; Borkhardt A
Hum Mutat; 2014 Oct; 35(10):1260-70. PubMed ID: 25066732
[TBL] [Abstract][Full Text] [Related]
5. Single-cell sequencing deciphers a convergent evolution of copy number alterations from primary to circulating tumor cells.
Gao Y; Ni X; Guo H; Su Z; Ba Y; Tong Z; Guo Z; Yao X; Chen X; Yin J; Yan Z; Guo L; Liu Y; Bai F; Xie XS; Zhang N
Genome Res; 2017 Aug; 27(8):1312-1322. PubMed ID: 28487279
[TBL] [Abstract][Full Text] [Related]
6. Genomic variations in plasma cell free DNA differentiate early stage lung cancers from normal controls.
Xia S; Huang CC; Le M; Dittmar R; Du M; Yuan T; Guo Y; Wang Y; Wang X; Tsai S; Suster S; Mackinnon AC; Wang L
Lung Cancer; 2015 Oct; 90(1):78-84. PubMed ID: 26233568
[TBL] [Abstract][Full Text] [Related]
7. Next-generation Sequencing (NGS) Analysis on Single Circulating Tumor Cells (CTCs) with No Need of Whole-genome Amplification (WGA).
Palmirotta R; Lovero D; Silvestris E; Felici C; Quaresmini D; Cafforio P; Silvestris F
Cancer Genomics Proteomics; 2017; 14(3):173-179. PubMed ID: 28446532
[TBL] [Abstract][Full Text] [Related]
8. Comparison of single cell sequencing data between two whole genome amplification methods on two sequencing platforms.
Chen D; Zhen H; Qiu Y; Liu P; Zeng P; Xia J; Shi Q; Xie L; Zhu Z; Gao Y; Huang G; Wang J; Yang H; Chen F
Sci Rep; 2018 Mar; 8(1):4963. PubMed ID: 29563514
[TBL] [Abstract][Full Text] [Related]
9. Massively parallel sequencing of micro-manipulated cells targeting a comprehensive panel of disease-causing genes: A comparative evaluation of upstream whole-genome amplification methods.
Deleye L; Gansemans Y; De Coninck D; Van Nieuwerburgh F; Deforce D
PLoS One; 2018; 13(4):e0196334. PubMed ID: 29698522
[TBL] [Abstract][Full Text] [Related]
10. Precision oncology using a limited number of cells: optimization of whole genome amplification products for sequencing applications.
Sho S; Court CM; Winograd P; Lee S; Hou S; Graeber TG; Tseng HR; Tomlinson JS
BMC Cancer; 2017 Jul; 17(1):457. PubMed ID: 28666423
[TBL] [Abstract][Full Text] [Related]
11. Genome-Wide Copy Number Alteration Detection in Preimplantation Genetic Diagnosis.
Deleye L; De Coninck D; Deforce D; Van Nieuwerburgh F
Methods Mol Biol; 2018; 1712():27-42. PubMed ID: 29224066
[TBL] [Abstract][Full Text] [Related]
12. The Performance of Whole Genome Amplification Methods and Next-Generation Sequencing for Pre-Implantation Genetic Diagnosis of Chromosomal Abnormalities.
Li N; Wang L; Wang H; Ma M; Wang X; Li Y; Zhang W; Zhang J; Cram DS; Yao Y
J Genet Genomics; 2015 Apr; 42(4):151-9. PubMed ID: 25953353
[TBL] [Abstract][Full Text] [Related]
13. Single-Cell Whole-Genome Amplification and Sequencing: Methodology and Applications.
Huang L; Ma F; Chapman A; Lu S; Xie XS
Annu Rev Genomics Hum Genet; 2015; 16():79-102. PubMed ID: 26077818
[TBL] [Abstract][Full Text] [Related]
14. Negative Enrichment and Isolation of Circulating Tumor Cells for Whole Genome Amplification.
Kanwar N; Done SJ
Methods Mol Biol; 2017; 1634():143-152. PubMed ID: 28819847
[TBL] [Abstract][Full Text] [Related]
15. Low-pass Whole-genome Sequencing of Circulating Cell-free DNA Demonstrates Dynamic Changes in Genomic Copy Number in a Squamous Lung Cancer Clinical Cohort.
Chen X; Chang CW; Spoerke JM; Yoh KE; Kapoor V; Baudo C; Aimi J; Yu M; Liang-Chu MMY; Suttmann R; Huw LY; Gendreau S; Cummings C; Lackner MR
Clin Cancer Res; 2019 Apr; 25(7):2254-2263. PubMed ID: 30617129
[TBL] [Abstract][Full Text] [Related]
16. A pipeline for copy number profiling of single circulating tumour cells to assess intrapatient tumour heterogeneity.
Deger T; Mendelaar PAJ; Kraan J; Prager-van der Smissen WJC; van der Vlugt-Daane M; Bindels EMJ; Sieuwerts AM; Sleijfer S; Wilting SM; Hollestelle A; Martens JWM
Mol Oncol; 2022 Aug; 16(16):2981-3000. PubMed ID: 34964258
[TBL] [Abstract][Full Text] [Related]
17. Massively parallel whole genome amplification for single-cell sequencing using droplet microfluidics.
Hosokawa M; Nishikawa Y; Kogawa M; Takeyama H
Sci Rep; 2017 Jul; 7(1):5199. PubMed ID: 28701744
[TBL] [Abstract][Full Text] [Related]
18. Genomic Analysis of Localized High-Risk Prostate Cancer Circulating Tumor Cells at the Single-Cell Level.
Rangel-Pozzo A; Liu S; Wajnberg G; Wang X; Ouellette RJ; Hicks GG; Drachenberg D; Mai S
Cells; 2020 Aug; 9(8):. PubMed ID: 32784507
[TBL] [Abstract][Full Text] [Related]
19. PCR-Free Shallow Whole Genome Sequencing for Chromosomal Copy Number Detection from Plasma of Cancer Patients Is an Efficient Alternative to the Conventional PCR-Based Approach.
Beagan JJ; Drees EEE; Stathi P; Eijk PP; Meulenbroeks L; Kessler F; Middeldorp JM; Pegtel DM; Zijlstra JM; Sie D; Heideman DAM; Thunnissen E; Smit L; de Jong D; Mouliere F; Ylstra B; Roemer MGM; van Dijk E
J Mol Diagn; 2021 Nov; 23(11):1553-1563. PubMed ID: 34454114
[TBL] [Abstract][Full Text] [Related]
20. Genomic analysis of Korean patients with advanced prostate cancer by use of a comprehensive next-generation sequencing panel and low-coverage, whole-genome sequencing.
Kang M; Cho E; Jang J; Lee J; Jeon Y; Jeong BC; Seo SI; Jeon SS; Lee HM; Choi HY; Jeon HG
Investig Clin Urol; 2019 Jul; 60(4):227-234. PubMed ID: 31294131
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
